Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SCHIFF REAGENT FUCHSIN-SULFUROUS ACID

K-Number: K842919 · 1984-09-11

Decision Date1984-09-11
Product CodeHZT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SCHIFF REAGENT FUCHSIN-SULFUROUS ACID is the device name listed in this FDA 510(k) record. The listed applicant is E K Ind., Inc.. It received FDA 510(k) clearance on 1984-09-11 under 510(k) number K842919. The device is classified under product code HZT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHIFF REAGENT FUCHSIN-SULFUROUS ACID?

SCHIFF REAGENT FUCHSIN-SULFUROUS ACID is a medical device that received FDA 510(k) clearance on 1984-09-11. The listed applicant is E K Ind., Inc.. The 510(k) number is K842919.

When did SCHIFF REAGENT FUCHSIN-SULFUROUS ACID receive FDA 510(k) clearance?

SCHIFF REAGENT FUCHSIN-SULFUROUS ACID received FDA 510(k) clearance on 1984-09-11, under 510(k) number K842919.

Who is the listed applicant for SCHIFF REAGENT FUCHSIN-SULFUROUS ACID?

The FDA 510(k) record lists E K Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCHIFF REAGENT FUCHSIN-SULFUROUS ACID?

The FDA product code for SCHIFF REAGENT FUCHSIN-SULFUROUS ACID is HZT.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing E K Ind., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 50 devices →

Related Devices (Code: HZT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑